A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218806



Internal ID22364032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:399282..452983hg38UCSC Ensembl
Outerchr10:445222..498923hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3853702
hg1953702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv699n152
Supporting Variantsnssv14277965, nssv14277966, nssv14277964
SamplesHG00512, HG00513, HG00514
Known GenesDIP2C
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218806
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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